de la cruz tincture of iodine

Generic: iodine and sodium iodide and alcohol

Labeler: dlc laboratories, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name de la cruz tincture of iodine
Generic Name iodine and sodium iodide and alcohol
Labeler dlc laboratories, inc.
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

alcohol 470 mg/mL, iodine 20 mg/mL, sodium iodide 20.4 mg/mL

Manufacturer
DLC Laboratories, Inc.

Identifiers & Regulatory

Product NDC 24286-1528
Product ID 24286-1528_0c940d4f-cca2-7175-e063-6394a90af568
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M003
Listing Expiration 2026-12-31
Marketing Start 1979-01-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 242861528
Hyphenated Format 24286-1528

Supplemental Identifiers

UPC
0324286153015
UNII
3K9958V90M 9679TC07X4 F5WR8N145C

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name de la cruz tincture of iodine (source: ndc)
Generic Name iodine and sodium iodide and alcohol (source: ndc)
Application Number M003 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 470 mg/mL
  • 20 mg/mL
  • 20.4 mg/mL
source: ndc
Packaging
  • 30 mL in 1 BOTTLE (24286-1528-7)
source: ndc

Packages (1)

Ingredients (3)

alcohol (470 mg/mL) iodine (20 mg/mL) sodium iodide (20.4 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0c940d4f-cca2-7175-e063-6394a90af568", "openfda": {"upc": ["0324286153015"], "unii": ["3K9958V90M", "9679TC07X4", "F5WR8N145C"], "spl_set_id": ["5d8f60a9-6d1c-0b0f-e053-2991aa0a8a9b"], "manufacturer_name": ["DLC Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (24286-1528-7)", "package_ndc": "24286-1528-7", "marketing_start_date": "20171027"}], "brand_name": "De La Cruz Tincture of Iodine", "product_id": "24286-1528_0c940d4f-cca2-7175-e063-6394a90af568", "dosage_form": "LIQUID", "product_ndc": "24286-1528", "generic_name": "Iodine and Sodium Iodide and Alcohol", "labeler_name": "DLC Laboratories, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "De La Cruz Tincture of Iodine", "active_ingredients": [{"name": "ALCOHOL", "strength": "470 mg/mL"}, {"name": "IODINE", "strength": "20 mg/mL"}, {"name": "SODIUM IODIDE", "strength": "20.4 mg/mL"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19790101", "listing_expiration_date": "20261231"}